WO2011041729A3 - Compounds as lysophosphatidic acid receptor antagonists - Google Patents

Compounds as lysophosphatidic acid receptor antagonists Download PDF

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Publication number
WO2011041729A3
WO2011041729A3 PCT/US2010/051199 US2010051199W WO2011041729A3 WO 2011041729 A3 WO2011041729 A3 WO 2011041729A3 US 2010051199 W US2010051199 W US 2010051199W WO 2011041729 A3 WO2011041729 A3 WO 2011041729A3
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WIPO (PCT)
Prior art keywords
compounds
receptor antagonists
acid receptor
lysophosphatidic acid
antagonists
Prior art date
Application number
PCT/US2010/051199
Other languages
French (fr)
Other versions
WO2011041729A2 (en
Inventor
Thomas Jon Seiders
Lucy Zhao
Jeannie M. Arruda
Brian Andrew Stearns
Yen Pham Truong
Jill Melissa Scott
John Howard Hutchinson
Nicholas Simon Stock
Deborah Volkots
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Amira Pharmaceuticals, Inc.
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Filing date
Publication date
Application filed by Amira Pharmaceuticals, Inc. filed Critical Amira Pharmaceuticals, Inc.
Priority to IN2177DEN2012 priority Critical patent/IN2012DN02177A/en
Priority to CN201080054528.7A priority patent/CN102666504B/en
Priority to EP10821369A priority patent/EP2483253A4/en
Priority to JP2012532368A priority patent/JP2013506695A/en
Publication of WO2011041729A2 publication Critical patent/WO2011041729A2/en
Publication of WO2011041729A3 publication Critical patent/WO2011041729A3/en

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
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    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D261/14Nitrogen atoms
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    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D261/18Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
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    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
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    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems

Abstract

Described herein are compounds that are antagonists of lysophosphatidic receptor(s). Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well as methods of using such antagonists, alone and in combination with other compounds, for treating LPA-dependent or LPA-mediated conditions or diseases.
PCT/US2010/051199 2009-10-01 2010-10-01 Compounds as lysophosphatidic acid receptor antagonists WO2011041729A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
IN2177DEN2012 IN2012DN02177A (en) 2009-10-01 2010-10-01
CN201080054528.7A CN102666504B (en) 2009-10-01 2010-10-01 Compound as lpa receptor antagonist
EP10821369A EP2483253A4 (en) 2009-10-01 2010-10-01 Compounds as lysophosphatidic acid receptor antagonists
JP2012532368A JP2013506695A (en) 2009-10-01 2010-10-01 Compounds as lysophosphatidic acid receptor antagonists

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US24786109P 2009-10-01 2009-10-01
US61/247,861 2009-10-01

Publications (2)

Publication Number Publication Date
WO2011041729A2 WO2011041729A2 (en) 2011-04-07
WO2011041729A3 true WO2011041729A3 (en) 2011-08-04

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ID=43128102

Family Applications (2)

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PCT/US2010/051150 WO2011041694A2 (en) 2009-10-01 2010-10-01 Compounds as lysophosphatidic acid receptor antagonists
PCT/US2010/051199 WO2011041729A2 (en) 2009-10-01 2010-10-01 Compounds as lysophosphatidic acid receptor antagonists

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Application Number Title Priority Date Filing Date
PCT/US2010/051150 WO2011041694A2 (en) 2009-10-01 2010-10-01 Compounds as lysophosphatidic acid receptor antagonists

Country Status (10)

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US (3) US8217066B2 (en)
EP (2) EP2483252B1 (en)
JP (2) JP2013506694A (en)
CN (2) CN102666504B (en)
AR (1) AR078497A1 (en)
GB (1) GB2474120B (en)
IN (2) IN2012DN02177A (en)
TW (1) TWI401082B (en)
UY (1) UY32926A (en)
WO (2) WO2011041694A2 (en)

Families Citing this family (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8455499B2 (en) 2008-12-11 2013-06-04 Amira Pharmaceuticals, Inc. Alkyne antagonists of lysophosphatidic acid receptors
GB2466121B (en) 2008-12-15 2010-12-08 Amira Pharmaceuticals Inc Antagonists of lysophosphatidic acid receptors
GB2470833B (en) 2009-06-03 2011-06-01 Amira Pharmaceuticals Inc Polycyclic antagonists of lysophosphatidic acid receptors
JP2013501064A (en) 2009-08-04 2013-01-10 アミラ ファーマシューティカルス,インコーポレーテッド Compounds as lysophosphatidic acid receptor antagonists
GB2474748B (en) * 2009-10-01 2011-10-12 Amira Pharmaceuticals Inc Polycyclic compounds as lysophosphatidic acid receptor antagonists
GB2474120B (en) 2009-10-01 2011-12-21 Amira Pharmaceuticals Inc Compounds as Lysophosphatidic acid receptor antagonists
AU2011338561A1 (en) 2010-12-07 2013-07-25 Amira Pharmaceuticals, Inc. Lysophosphatidic acid receptor antagonists and their use in the treatment of fibrosis
WO2012138797A1 (en) 2011-04-05 2012-10-11 Amira Pharmaceuticals, Inc. 3- or 5 - bi phenyl - 4 - ylisoxazole - based compounds useful for the treatment of fibrosis, pain, cancer and respiratory, allergic, nervous system or cardiovascular disorders
WO2013020622A1 (en) * 2011-08-08 2013-02-14 Merck Patent Gmbh N-(benzimimdazol-2-yl)-cyclopropane carboxamides as lysophosphatidic acid antagonists
CN104066729A (en) 2011-08-15 2014-09-24 英特穆恩公司 Lysophosphatidic acid receptor antagonists
WO2013070879A1 (en) * 2011-11-10 2013-05-16 Bristol-Myers Squibb Company Methods for treating spinal cord injury with lpa receptor antagonists
EP2783016A1 (en) 2011-11-22 2014-10-01 Intermune, Inc. Methods of diagnosing and treating idiopathic pulmonary fibrosis
US9447078B2 (en) 2012-01-20 2016-09-20 Acucela Inc. Substituted heterocyclic compounds for disease treatment
WO2014104372A1 (en) 2012-12-28 2014-07-03 宇部興産株式会社 Halogen-substituted heterocyclic compound
WO2014159814A1 (en) * 2013-03-13 2014-10-02 Patricia Oliver Formulations and tablets for treatment or prevention of neurological disorders
WO2014145873A2 (en) * 2013-03-15 2014-09-18 Epigen Biosciences, Inc. Heterocyclic compounds useful in the treatment of disease
EA038294B1 (en) * 2013-05-24 2021-08-05 Эпиджен Байосайенсиз, Инк. Heterocyclic compounds useful in the treatment of diseases
CN105873907B (en) 2013-12-05 2019-03-12 拜耳作物科学股份公司 N- naphthenic base-N- { [2- (naphthenic base that 1- replaces) phenyl] methylene }-(thio) carboxamides derivatives
CN105793243A (en) 2013-12-05 2016-07-20 拜耳作物科学股份公司 N-cycloalkyl-n-{[2-(1-substitutedcycloalkyl)phenyl]methylene}-(thio)carboxamide derivatives
AU2015229188A1 (en) 2014-03-13 2016-09-29 Proteostasis Therapeutics, Inc. Compounds, compositions, and methods for increasing CFTR activity
EP3116870A1 (en) 2014-03-13 2017-01-18 Proteostasis Therapeutics, Inc. Compounds, compositions, and methods for increasing cftr activity
EP3157917B1 (en) 2014-06-19 2020-03-18 Proteostasis Therapeutics, Inc. Compounds, compositions and methods of increasing cftr activity
CN106458964B (en) 2014-06-27 2019-11-22 宇部兴产株式会社 The salt of halogen substituted heterocyclic compound
MA41253A (en) 2014-12-23 2017-10-31 Proteostasis Therapeutics Inc COMPOUNDS, COMPOSITIONS AND PROCESSES TO INCREASE THE ACTIVITY OF CFTR
WO2016105468A1 (en) 2014-12-23 2016-06-30 Proteostasis Therapeutics, Inc. Derivatives of 3-heteroarylisoxazol-5-carboxylic amide useful for the treatment of inter alia cystic fibrosis
CA2971855A1 (en) 2014-12-23 2016-06-30 Proteostasis Therapeutics, Inc. Derivatives of 5-(hetero)arylpyrazol-3-carboxylic amide or 1-(hetero)aryltriazol-4-carboxylic amide useful for the treatment of inter alia cystic fibrosis
WO2016105477A1 (en) 2014-12-23 2016-06-30 Proteostasis Therapeutics, Inc Derivatives of 5-phenyl- or 5-heteroarylthiazol-2-carboxylic amide useful for the treatment of inter alia cystic fibrosis
JP6929792B2 (en) 2015-02-16 2021-09-01 ザ ユニバーシティ オブ クィーンズランド Sulfonylureas and related compounds and their use
CA2988306A1 (en) 2015-06-05 2016-12-08 Vertex Pharmaceuticals Incorporated Triazoles for the treatment of demyelinating diseases
AU2016297886B2 (en) 2015-07-24 2020-12-10 Proteostasis Therapeutics, Inc. Compounds, compositions and methods of increasing CFTR activity
BR112018007021B1 (en) 2015-10-06 2024-01-09 Proteostasis Therapeutics, Inc Compound, composition comprising said compounds and use thereof to treat cystic fibrosis
MA43775A (en) 2016-04-07 2021-05-05 Proteostasis Therapeutics Inc ANALOGUES OF IVACAFTOR CONTAINING SILICON ATOMS
AU2017280206A1 (en) 2016-06-21 2019-01-17 Proteostasis Therapeutics, Inc. Compounds, compositions, and methods for increasing CFTR activity
AR108838A1 (en) 2016-06-21 2018-10-03 Bristol Myers Squibb Co CARBAMOYLOXIMETHYL ACID TRIAZOL CYCLOHEXILO AS LPA ANTAGONISTS
WO2018106646A1 (en) 2016-12-06 2018-06-14 Vertex Pharmaceuticals Incorporated Aminotriazoles for the treatment of demyelinating diseases
WO2018106641A1 (en) 2016-12-06 2018-06-14 Vertex Pharmaceuticals Incorporated Pyrazoles for the treatment of demyelinating diseases
WO2018106643A1 (en) 2016-12-06 2018-06-14 Vertex Pharmaceuticals Incorporated Heterocyclic azoles for the treatment of demyelinating diseases
US10961242B2 (en) 2017-05-17 2021-03-30 Legochem Biosciences, Inc. Compounds as autotaxin inhibitors and pharmaceutical compositions comprising the same
KR101798840B1 (en) 2017-05-17 2017-11-17 주식회사 레고켐 바이오사이언스 Novel Compounds as Autotaxin Inhibitors and Pharmaceutical Compositions Comprising the Same
RS62910B1 (en) 2017-07-07 2022-03-31 Inflazome Ltd Novel sulfonamide carboxamide compounds
US11370776B2 (en) 2017-07-07 2022-06-28 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
RU2020110219A (en) * 2017-08-15 2021-09-17 Инфлазоум Лимитед SULFONYLUREAS AND SULFONYLTHIUREAS AS NLRP3 INHIBITORS
US11542255B2 (en) 2017-08-15 2023-01-03 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
US11926600B2 (en) 2017-08-15 2024-03-12 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
RU2020110366A (en) * 2017-08-15 2021-09-16 Инфлазоум Лимитед NEW COMPOUNDS OF SULFONAMIDE CARBOXAMIDES
WO2019041340A1 (en) * 2017-09-04 2019-03-07 Eli Lilly And Company Lysophosphatidic acid receptor 1 (lpar1) inhibitor compounds
US11319315B2 (en) 2017-12-19 2022-05-03 Bristol-Myers Squibb Company Cyclohexyl acid triazole azoles as LPA antagonists
KR20200100753A (en) 2017-12-19 2020-08-26 브리스톨-마이어스 스큅 컴퍼니 Cyclohexyl acid pyrazole azole as an LPA antagonist
KR20200100722A (en) 2017-12-19 2020-08-26 브리스톨-마이어스 스큅 컴퍼니 Cyclohexyl acid isoxazole azine as an LPA antagonist
WO2019126087A1 (en) * 2017-12-19 2019-06-27 Bristol-Myers Squibb Company Cyclohexyl acid isoxazole azoles as lpa antagonists
JP7208240B2 (en) 2017-12-19 2023-01-18 ブリストル-マイヤーズ スクイブ カンパニー Cyclohexylate triazole azines as LPA antagonists
CN112041304A (en) 2017-12-19 2020-12-04 百时美施贵宝公司 Isoxazole N-linked carbamoylcyclohexanoic acids as LPA antagonists
US11261174B2 (en) 2017-12-19 2022-03-01 Bristol-Myers Squibb Company Pyrazole O-linked carbamoyl cyclohexyl acids as LPA antagonists
KR20200101957A (en) 2017-12-19 2020-08-28 브리스톨-마이어스 스큅 컴퍼니 Isoxazole O-linked carbamoyl cyclohexyl acid as LPA antagonist
EA202091500A1 (en) 2017-12-19 2020-09-14 Бристол-Маерс Сквибб Компани Pyrazole N-Bonded Carbamoylcyclohexyl Acids as LPA Antagonists
CN112189010A (en) 2017-12-19 2021-01-05 百时美施贵宝公司 Triazole N-linked carbamoylcyclohexanoic acids as LPA antagonists
CN112055710A (en) 2017-12-19 2020-12-08 百时美施贵宝公司 Cyclohexyl acid pyrazole azines as LPA antagonists
US11905252B2 (en) 2018-03-02 2024-02-20 Inflazome Limited Compounds
CA3046894A1 (en) * 2018-06-18 2019-12-18 Epigen Biosciences, Inc. Heterocyclic compounds useful in the treatment of disease
MX2022001264A (en) * 2019-07-30 2022-02-22 Taisho Pharmaceutical Co Ltd Urea compound for antagonizing lpa1 receptor.
CA3158743A1 (en) 2019-11-15 2021-05-20 Gilead Sciences, Inc. Triazole carbamate pyridyl sulfonamides as lpa receptor antagonists and uses thereof
TW202134213A (en) * 2019-11-29 2021-09-16 日商小野藥品工業股份有限公司 Compound having lysophosphatidic acid receptor agonistic activity and pharmaceutical use of said compound
US11702407B2 (en) 2020-06-03 2023-07-18 Gilead Sciences, Inc. LPA receptor antagonists and uses thereof
TW202344504A (en) 2020-06-03 2023-11-16 美商基利科學股份有限公司 Lpa receptor antagonists and uses thereof
US11939318B2 (en) 2021-12-08 2024-03-26 Gilead Sciences, Inc. LPA receptor antagonists and uses thereof
TW202342017A (en) 2022-02-25 2023-11-01 美商洛子峰生物有限公司 Compounds and compositions for treating conditions associated with lpa receptor activity
CN114907282B (en) * 2022-05-24 2023-08-22 华南理工大学 Method for synthesizing 4-phenyl alkenyl isoxazole derivative
CN117126044B (en) * 2023-04-12 2024-01-26 延边大学 Microwave-assisted synthesis method of methyl ketone compound

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030114505A1 (en) * 2000-02-18 2003-06-19 Akihiro Ueno Novel isoxazole and thiazole compounds and use thereof as drugs
EP1340749A1 (en) * 2000-11-17 2003-09-03 Takeda Chemical Industries, Ltd. Isoxazole derivatives
JP2003261545A (en) * 2001-12-28 2003-09-19 Takeda Chem Ind Ltd Neurotrophic factor production/secretion accelerator

Family Cites Families (77)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4229447A (en) 1979-06-04 1980-10-21 American Home Products Corporation Intraoral methods of using benzodiazepines
US4476116A (en) 1982-12-10 1984-10-09 Syntex (U.S.A.) Inc. Polypeptides/chelating agent nasal compositions having enhanced peptide absorption
US5116817A (en) 1982-12-10 1992-05-26 Syntex (U.S.A.) Inc. LHRH preparations for intranasal administration
US4596795A (en) 1984-04-25 1986-06-24 The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives
DE3684446D1 (en) 1985-12-28 1992-04-23 Sumitomo Pharma MEDICINAL PRODUCTS WITH DELAYED RELEASED RELEASE.
US4755386A (en) 1986-01-22 1988-07-05 Schering Corporation Buccal formulation
JP2633641B2 (en) 1988-08-26 1997-07-23 本田技研工業株式会社 Exhaust gas concentration detector
US5739136A (en) 1989-10-17 1998-04-14 Ellinwood, Jr.; Everett H. Intraoral dosing method of administering medicaments
US5017381A (en) 1990-05-02 1991-05-21 Alza Corporation Multi-unit pulsatile delivery system
US5229135A (en) 1991-11-22 1993-07-20 Prographarm Laboratories Sustained release diltiazem formulation
US5612359A (en) 1994-08-26 1997-03-18 Bristol-Myers Squibb Company Substituted biphenyl isoxazole sulfonamides
JPH096712A (en) 1995-06-23 1997-01-10 Canon Inc Data processor
GB9523946D0 (en) 1995-11-23 1996-01-24 Bayer Ag Leukotriene antagonistic benzoic acid derivatives
US5837284A (en) 1995-12-04 1998-11-17 Mehta; Atul M. Delivery of multiple doses of medications
ATE236890T1 (en) 1996-12-23 2003-04-15 Bristol Myers Squibb Pharma Co OXYGEN OR SULFUR CONTAINING 5-MEMBED HETEROAROMATIC DERIVATIVES AS FACTOR XA INHIBITORS
JP3237608B2 (en) 1997-04-21 2001-12-10 住友製薬株式会社 Isoxazole derivative
US5840329A (en) 1997-05-15 1998-11-24 Bioadvances Llc Pulsatile drug delivery system
US6391452B1 (en) 1997-07-18 2002-05-21 Bayer Corporation Compositions for nasal drug delivery, methods of making same, and methods of removing residual solvent from pharmaceutical preparations
CA2368630A1 (en) 1999-04-02 2000-10-12 Ruth R. Wexler Aryl sulfonyls as factor xa inhibitors
DE10013485C1 (en) 2000-03-18 2001-07-12 Krupp Bilstein Gmbh Vehicle lifting jack has cog segment of pivoted carrier arm cooperating with cog section of control slider displaced parallel to support column
JPWO2001072723A1 (en) 2000-03-28 2004-01-08 日本曹達株式会社 Oxa (thia) zolidine derivatives and anti-inflammatory drugs
WO2002000651A2 (en) 2000-06-27 2002-01-03 Bristol-Myers Squibb Pharma Company Factor xa inhibitors
DE60234318D1 (en) 2001-02-08 2009-12-24 Ono Pharmaceutical Co FOR THE TREATMENT OF RESPIRATORY DISEASES, COMPRISING MEANS FOR THE CONTROL OF THE LPA RECEPTOR
US7521192B2 (en) 2001-04-18 2009-04-21 Rigel Pharmaceuticals, Inc. EDG: modulators of lymphocyte activation and migration
ES2312588T3 (en) 2001-07-17 2009-03-01 Ono Pharmaceutical Co., Ltd. REGULATION OF THE PANCREATIC JUICE SECRETION UNDERSTANDING A LPA RECEIVER REGULATION AGENT.
MY151199A (en) 2001-11-02 2014-04-30 Rigel Pharmaceuticals Inc Substituted diphenyl heterocycles useful for treating hcv infection
JP4569106B2 (en) 2001-12-25 2010-10-27 味の素株式会社 Organ fibrosis inhibitor
EP1513522A2 (en) 2002-01-18 2005-03-16 Sri International Methods of treating conditions associated with an edg receptor
US20050101518A1 (en) 2002-01-18 2005-05-12 David Solow-Cordero Methods of treating conditions associated with an EDG-2 receptor
US20050113283A1 (en) 2002-01-18 2005-05-26 David Solow-Cordero Methods of treating conditions associated with an EDG-4 receptor
US20050261298A1 (en) 2002-01-18 2005-11-24 David Solow-Cordero Methods of treating conditions associated with an Edg-7 receptor
JP4547912B2 (en) 2002-03-05 2010-09-22 小野薬品工業株式会社 8-Azaprostaglandin derivative compound and drug containing the compound as an active ingredient
WO2003094965A2 (en) 2002-05-08 2003-11-20 Neuronova Ab Modulation of neural stem cells with s1p or lpa receptor agonists
JP2005529923A (en) 2002-05-13 2005-10-06 イーライ・リリー・アンド・カンパニー Polycyclic compounds for use as melanin-concentrating hormone antagonists in the treatment of obesity and diabetes
AU2003241833A1 (en) 2002-05-28 2003-12-12 Ono Pharmaceutical Co., Ltd. Beta-ALANINE DERIVATIVE AND USE THEREOF
EP1550461A1 (en) 2002-06-26 2005-07-06 Ono Pharmaceutical Co., Ltd. Remedy for chronic disease
JP4691988B2 (en) 2002-10-03 2011-06-01 小野薬品工業株式会社 LPA receptor antagonist
PL376971A1 (en) 2002-11-19 2006-01-23 Amgen, Inc. Amplified genes involved in cancer
US20040192739A1 (en) 2003-01-16 2004-09-30 David Solow-Cordero Methods of treating conditions associated with an Edg-2 receptor
US20050065194A1 (en) 2003-01-16 2005-03-24 Geetha Shankar Methods of treating conditions associated with an Edg-2 receptor
US20040167132A1 (en) 2003-01-16 2004-08-26 Geetha Shankar Methods of treating conditions associted with an Edg-2 receptor
US7135469B2 (en) 2003-03-18 2006-11-14 Bristol Myers Squibb, Co. Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors
US20060089398A1 (en) * 2003-03-19 2006-04-27 Gang Liu Isoxazole carboxamide derivatives as ghrelin receptor modulators
US7115642B2 (en) 2003-05-02 2006-10-03 Rigel Pharmaceuticals, Inc. Substituted diphenyl isoxazoles, pyrazoles and oxadiazoles useful for treating HCV infection
PL1638551T3 (en) 2003-05-19 2012-05-31 Irm Llc Immunosuppressant compounds and compositions
WO2005012269A1 (en) 2003-08-05 2005-02-10 Ajinomoto Co., Inc. Novel azole compound
ATE528276T1 (en) 2003-12-19 2011-10-15 Ono Pharmaceutical Co LYSOPHOSPHATIDYL ACID RECEPTOR ANTAGONIST COMPOUNDS AND THEIR APPLICATIONS
DE10360369A1 (en) 2003-12-22 2005-07-14 Bayer Cropscience Ag amides
WO2005123671A1 (en) 2004-06-22 2005-12-29 Taisho Pharmaceutical Co., Ltd. Pyrrole derivative
US7405237B2 (en) * 2004-07-28 2008-07-29 Celgene Corporation Isoindoline compounds and methods of their use
JP2006096712A (en) 2004-09-30 2006-04-13 Senju Pharmaceut Co Ltd Corneal sensitivity improver containing lpa receptor antagonist
AR055041A1 (en) 2005-03-23 2007-08-01 Merck Frosst Canada Ltd TIADIAZOLS AND OXADIAZOLS AS INHIBITORS OF THE SYNTHESIS OF LEUCOTRIENOS. PHARMACEUTICAL COMPOSITIONS.
WO2006131336A1 (en) 2005-06-08 2006-12-14 Novartis Ag POLYCYCLIC OXADIAZOLES OR I SOXAZOLES AND THEIR USE AS SlP RECEPTOR LIGANDS
WO2007007588A1 (en) 2005-07-08 2007-01-18 Ono Pharmaceutical Co., Ltd. Compound having cyclic group with planarity as core
AU2006279211A1 (en) 2005-08-11 2007-02-15 Merck Frosst Canada Ltd Novel substituted 1,2,3-triazolylmethyl-benzothiophene or -indole and their use as leukotriene biosynthesis inhibitors
JP2009506046A (en) 2005-08-23 2009-02-12 アイアールエム・リミテッド・ライアビリティ・カンパニー Immunosuppressant compounds and compositions
US7405302B2 (en) 2005-10-11 2008-07-29 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (FLAP) inhibitors
US20070219206A1 (en) 2005-11-04 2007-09-20 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (flap) inhibitors
US7977359B2 (en) 2005-11-04 2011-07-12 Amira Pharmaceuticals, Inc. 5-lipdxygenase-activating protein (FLAP) inhibitors
US20070225285A1 (en) 2005-11-04 2007-09-27 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (flap) inhibitors
CA2636043A1 (en) 2006-01-23 2007-08-02 Amira Pharmaceuticals, Inc. Tricyclic inhibitors of 5-lipoxygenase
CA2643670A1 (en) 2006-02-27 2007-08-30 Sterix Limited Diaryl compounds as non-steroidal inhibitors of 17-beta hydroxysteroid dehydrogenase and/or steroid sulphatase for the treatment of oestrogen-related diseases such as hormone dependent breast cancer
US20090029949A1 (en) 2006-05-25 2009-01-29 Parrill-Baker Abby L GPCR Ligands Identified by Computational Modeling
WO2008024979A2 (en) 2006-08-24 2008-02-28 The Scripps Research Institute Methods utilizing cell-signaling lysophospholipids
US20080051372A1 (en) 2006-08-24 2008-02-28 The Scripps Research Institute Methods utilizing cell-signaling lysophospholipids
WO2008112201A2 (en) 2007-03-12 2008-09-18 The General Hospital Corporation Lysophosphatidic acid receptor targeting for lung disease
US9163091B2 (en) 2007-05-30 2015-10-20 Lpath, Inc. Compositions and methods for binding lysophosphatidic acid
US20090069288A1 (en) 2007-07-16 2009-03-12 Breinlinger Eric C Novel therapeutic compounds
SI2303270T1 (en) 2008-05-05 2018-01-31 Sanofi Acylamino-substituted fused cyclopentanecarboxylic acid derivatives and their use as pharmaceuticals
JP4933512B2 (en) 2008-10-09 2012-05-16 住友化学株式会社 Light guide plate
US8455499B2 (en) 2008-12-11 2013-06-04 Amira Pharmaceuticals, Inc. Alkyne antagonists of lysophosphatidic acid receptors
GB2466121B (en) 2008-12-15 2010-12-08 Amira Pharmaceuticals Inc Antagonists of lysophosphatidic acid receptors
GB2470833B (en) 2009-06-03 2011-06-01 Amira Pharmaceuticals Inc Polycyclic antagonists of lysophosphatidic acid receptors
JP2013501064A (en) 2009-08-04 2013-01-10 アミラ ファーマシューティカルス,インコーポレーテッド Compounds as lysophosphatidic acid receptor antagonists
GB2474120B (en) 2009-10-01 2011-12-21 Amira Pharmaceuticals Inc Compounds as Lysophosphatidic acid receptor antagonists
WO2011041551A1 (en) * 2009-10-01 2011-04-07 Intermune, Inc. Therapeutic antiviral peptides
GB2474748B (en) * 2009-10-01 2011-10-12 Amira Pharmaceuticals Inc Polycyclic compounds as lysophosphatidic acid receptor antagonists

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030114505A1 (en) * 2000-02-18 2003-06-19 Akihiro Ueno Novel isoxazole and thiazole compounds and use thereof as drugs
EP1340749A1 (en) * 2000-11-17 2003-09-03 Takeda Chemical Industries, Ltd. Isoxazole derivatives
JP2003261545A (en) * 2001-12-28 2003-09-19 Takeda Chem Ind Ltd Neurotrophic factor production/secretion accelerator

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
MASAHIKO KAINUMA ET AL: "Design, synthesis, and evaluation of non-steroidal farnesoid X receptor (FXR) antagonist", BIOORGANIC & MEDICINAL CHEMISTRY, vol. 15, no. 7, 2007, pages 2587 - 2600, XP005922449 *
See also references of EP2483253A4 *

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